He Xiaomin, Feng Bei, Huang Chuanpei, Wang Hao, Ge Yang, Hu Renjie, Yin Meng, Xu Zhiwei, Wang Wei, Fu Wei, Zheng Jinghao
Department of Pediatric Cardiothoracic Surgery, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Department of Pediatric Cardiothoracic Surgery, Shanghai Jiao Tong University, Shanghai, People's Republic of China ; Institute of Pediatric Translational Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Int J Nanomedicine. 2015 Mar 17;10:2089-99. doi: 10.2147/IJN.S79461. eCollection 2015.
Electrospinning has recently received considerable attention, showing notable potential as a novel method of scaffold fabrication for cartilage engineering. The aim of this study was to use a coculture strategy of chondrocytes combined with electrospun gelatin/polycaprolactone (GT/PCL) membranes, instead of pure chondrocytes, to evaluate the formation of cartilaginous tissue. We prepared the GT/PCL membranes, seeded bone marrow stromal cell (BMSC)/chondrocyte cocultures (75% BMSCs and 25% chondrocytes) in a sandwich model in vitro, and then implanted the constructs subcutaneously into nude mice for 12 weeks. Gross observation, histological and immunohistological evaluation, glycosaminoglycan analyses, Young's modulus measurement, and immunofluorescence staining were performed postimplantation. We found that the coculture group formed mature cartilage-like tissue, with no statistically significant difference from the chondrocyte group, and labeled BMSCs could differentiate into chondrocyte-like cells under the chondrogenic niche of chondrocytes. This entire strategy indicates that GT/PCL membranes are also a suitable scaffold for stem cell-based cartilage engineering and may provide a potentially clinically feasible approach for cartilage repairs.
静电纺丝法近来备受关注,作为一种用于软骨工程支架制造的新方法显示出显著潜力。本研究的目的是采用软骨细胞与静电纺丝明胶/聚己内酯(GT/PCL)膜的共培养策略,而非单纯的软骨细胞,来评估软骨组织的形成。我们制备了GT/PCL膜,在体外以三明治模型接种骨髓间充质干细胞(BMSC)/软骨细胞共培养物(75%BMSC和25%软骨细胞),然后将构建体皮下植入裸鼠体内12周。植入后进行大体观察、组织学和免疫组织学评估、糖胺聚糖分析、杨氏模量测量以及免疫荧光染色。我们发现共培养组形成了成熟的软骨样组织,与软骨细胞组相比无统计学显著差异,并且标记的BMSC在软骨细胞的软骨形成微环境下可分化为软骨样细胞。这一整体策略表明,GT/PCL膜也是基于干细胞的软骨工程的合适支架,可能为软骨修复提供一种潜在的临床可行方法。